Cefuroxime Axetil

CHEMBL1095930 Phase 4 Aprovado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
510.5 g/mol
LogP
0.9
Phase
4

The oral prodrug formulation of cefuroxime is hydrolyzed in the intestinal mucosa to release active cefuroxime. It is used for the outpatient treatment of mild to moderate infections including sinusitis, bronchitis, and urinary tract infections. It should be taken with food to maximize bioavailability.

Peso Molecular

510,5000 g/mol

LogP

0,90

TPSA

214,00 Ų

Regra dos 5 de Lipinski

Reprovado

Áreas Terapêuticas

Mecanismo de Ação

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Estrutura 2D

SVG PNG

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SMILES

CO/N=C(\C(=O)N[C@@H]1C(=O)N2C(C(=O)OC(C)OC(C)=O)=C(COC(N)=O)CS[C@H]12)c1ccco1

InChI

InChI=1S/C20H22N4O10S/c1-9(25)33-10(2)34-19(28)15-11(7-32-20(21)29)8-35-18-14(17(27)24(15)18)22-16(26)13(23-30-3)12-5-4-6-31-12/h4-6,10,14,18H,7-8H2,1-3H3,(H2,21,29)(H,22,26)/b23-13-/t10?,14-,18-/m1/s1

Molecular Formula

C20H22N4O10S

HBD / HBA

2 / 12

Ligações Rotacionáveis

12

Átomos Pesados

35

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Perguntas frequentes

The oral prodrug formulation of cefuroxime is hydrolyzed in the intestinal mucosa to release active cefuroxime. It is used for the outpatient treatment of mild to moderate infections including sinusitis, bronchitis, and urinary tract infections. It should be taken with food to maximize bioavailability.

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Yes, Cefuroxime Axetil is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1095930. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6321416. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Aviso Médico

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.